Guss R B, McCulley J P
Ann Ophthalmol. 1982 Nov;14(11):1058-60.
Wiskott-Aldrich syndrome is an x-linked disorder characterized by a triad of thrombocytopenia, eczema, and recurrent infections. Until recently, survival into the second decade was rare. In the last few years, a better understanding of the syndrome has been achieved, and earlier recognition and newer modes of treatment have improved life. These patients are living longer and ophthalmologic presentation reflects this change. We present three case histories of patients followed for the past 15 years who have had, in association with this syndrome, eczema of the eyelids, episcleritis, marginal keratitis, and blepharitis.
威斯科特-奥尔德里奇综合征是一种X连锁疾病，其特征为血小板减少、湿疹和反复感染三联征。直到最近，活到第二个十年的情况还很罕见。在过去几年里，对该综合征有了更好的认识，早期识别和新的治疗方式改善了患者的生活。这些患者寿命延长，眼科表现也反映了这一变化。我们呈现三例患者的病史，他们在过去15年里一直接受随访，患有与该综合征相关的眼睑湿疹、巩膜炎、边缘性角膜炎和睑缘炎。
